PinnedFormedixHow can automated metadata management help streamline your clinical trials?When it comes to efficient clinical study build, content is king. Most importantly: metadata content. Metadata is the building blocks of…Sep 28, 2023Sep 28, 2023
PinnedFormedixStreamlining Drug Development: the Role of CDISC StandardsThe clinical trial process is a long, expensive, complicated one that often ends in failure. That means to have a successful outcome…Jun 21, 2023Jun 21, 2023
FormedixWhat to consider when designing your CRFs in clinical trialsLearn the basics of CRFs, common design challenges, and our best practice approach for creating quality electronic case report forms.Jan 17Jan 17
FormedixAll you need to know about NCI, CDISC and SDTM controlled terminologyThe use of controlled terminology (CT) is vital to successful clinical study build, however, understanding the concept and its various…Dec 20, 2023Dec 20, 2023
FormedixSDTM supplemental qualifiers explained | FormedixWhat are SDTM supplemental qualifiers? In short, these are variables in non-CDISC datasets that cannot be mapped to a variable that matches…Nov 8, 2023Nov 8, 2023
FormedixWhat CDISC standards are used in clinical research? | FormedixThe Clinical Data Interchange Standards Consortium (CDISC) is dedicated to helping improve medical research through data standardization…Aug 16, 2023Aug 16, 2023
Formedix3 key facts about ADaM standards in clinical trialsOne of the most important standards when it comes to clinical trial submission is the Analysis Data Model (ADaM). ADaM standards outline…Jul 19, 2023Jul 19, 2023
